Skip to Content
MilliporeSigma
All Photos(1)

Documents

59891

Sigma-Aldrich

N-Acetyl-DL-β-phenylalanine

≥97.0% (HPLC)

Synonym(s):

Hydrocinnamic acid, (±)-3-(Acetylamino)-3-phenylpropionic acid

Sign Into View Organizational & Contract Pricing


About This Item

Empirical Formula (Hill Notation):
C11H13NO3
CAS Number:
Molecular Weight:
207.23
Beilstein/REAXYS Number:
2726794
MDL number:
UNSPSC Code:
12352200
PubChem Substance ID:

assay

≥97.0% (HPLC)

application(s)

peptide synthesis

SMILES string

CC(=O)NC(CC(O)=O)c1ccccc1

InChI

1S/C11H13NO3/c1-8(13)12-10(7-11(14)15)9-5-3-2-4-6-9/h2-6,10H,7H2,1H3,(H,12,13)(H,14,15)

InChI key

HTWAFOFDKZAKQP-UHFFFAOYSA-N

Biochem/physiol Actions

N-Acetyl-β-phenylalanine is a substrate for bacterial tRNA(Phe) peptidyltransferase. Hydrocinnamic acid is an aromatic lignin monomer.
N-Acetyl-DL-β-phenylalanine is a racemic mixture of N-acetylated β-phenylalanine enantiomers. N-Acetyl-DL-β-phenylalanine is a product generated from the chromogenic substrate N-acetyl-DL-phenylalanine β-napthyl ester by specific esterase(s).

Storage Class

13 - Non Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)


Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Anthony L Schilmiller et al.
The Plant journal : for cell and molecular biology, 60(5), 771-782 (2009-08-18)
The initial reactions of the phenylpropanoid pathway convert phenylalanine to p-coumaroyl CoA, a branch point metabolite from which many phenylpropanoids are made. Although the second enzyme of this pathway, cinnamic acid 4-hydroxylase (C4H), is well characterized, a mutant for the
T G Heckler et al.
Biochemistry, 27(19), 7254-7262 (1988-09-20)
Eight structurally modified peptidyl-tRNA(Phe),s were employed to study P-site binding and peptide bond formation in a cell-free system involving Escherichia coli ribosomes programmed with poly(uridylic acid). It was found that the two analogues (N-acetyl-D-phenylalanyl-tRNA(Phe) and N-acetyl-D-tyrosyl-tRNA(Phe] containing D-amino acids functioned
Heather D Coleman et al.
Proceedings of the National Academy of Sciences of the United States of America, 105(11), 4501-4506 (2008-03-05)
p-Coumaroyl-CoA 3'-hydroxylase (C3'H) is a cytochrome P450-dependent monooxygenase that catalyzes the 3'-hydroxylation of p-coumaroyl shikimate and p-coumaroyl quinate. We used RNA interference to generate transgenic hybrid poplar suppressed in C3'H expression and analyzed them with respect to transcript abundance, cell
P K Tsung et al.
Biochimica et biophysica acta, 445(1), 112-117 (1976-08-12)
The chemotactic and N-acetyl-DL-phenylalanine beta-naphthyl esterase activities of rabbit peritoneal neutrophils are separable from each other by both DEAE cellulose and Sephadex G-100 column chromatography. Partially purified esterase obtained from DEAE-cellulose chromatography had molecular weight of 70 000. However, the
Jae-Jung Ko et al.
Bioresource technology, 100(4), 1622-1627 (2008-11-04)
This study is designed to investigate the biodegradation of high molecular weight (HMW) lignin under sulfate reducing conditions. With a continuously mesophilic operated reactor in the presence of co-substrates of cellulose, the changes in HMW lignin concentration and chemical structure

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service